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Author/Creator Percy, Alan K.

1. Analysis of X‐inactivation status in a Rett syndrome natural history study cohort. Issue 5 (23rd March 2022)

Authors:
Fang, Xiaolan; Butler, Kameryn M.; Abidi, Fatima; Gass, Jennifer; Beisang, Arthur; Feyma, Timothy; Ryther, Robin C.; Standridge, Shannon; Heydemann, Peter; Jones, Mary; Haas, Richard; Lieberman, David N; Marsh, Eric D.; Benke, Tim A.; Skinner, Steve; Neul, Jeffrey L.; Percy, Alan K.; Friez, ...
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 10:Issue 5(2022)
Page Start:
n/a
Record Type:
Journal Article
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3. Characterizing the phenotypic effect of Xq28 duplication size in MECP2 duplication syndrome. Issue 5 (15th March 2019)

Authors:
Peters, Sarika U.; Fu, Cary; Suter, Bernhard; Marsh, Eric; Benke, Timothy A.; Skinner, Steve A.; Lieberman, David N.; Standridge, Shannon; Jones, Mary; Beisang, Arthur; Feyma, Timothy; Heydeman, Peter; Ryther, Robin; Kaufmann, Walter E.; Glaze, Daniel G.; Neul, Jeffrey L.; Percy, Alan K.
Journal:
Clinical genetics
Issue:
Volume 95:Issue 5(2019)
Page Start:
575
Record Type:
Journal Article
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4. Detection of rarely identified multiple mutations in MECP2 gene do not contribute to enhanced severity in rett syndrome. Issue 7 (21st May 2013)

Authors:
Chapleau, Christopher A.; Lane, Jane; Kirwin, Susan M.; Schanen, Carolyn; Vinette, Kathy M.B.; Stubbolo, Danielle; MacLeod, Patrick; Percy, Alan K.
Journal:
American journal of medical genetics
Issue:
Volume 161:Issue 7(2013:Jul.)
Page Start:
1638
Record Type:
Journal Article
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5. Double-blind, randomized, placebo-controlled study of trofinetide in pediatric Rett syndrome. (16th April 2019)

Authors:
Glaze, Daniel G.; Neul, Jeffrey L.; Kaufmann, Walter E.; Berry-Kravis, Elizabeth; Condon, Sean; Stoms, George; Oosterholt, Sean; Della Pasqua, Oscar; Glass, Larry; Jones, Nancy E.; Percy, Alan K.; Glaze, Daniel G.; Neul, Jeffrey L.; Kaufmann, Walter E.; Berry-Kravis, Elizabeth; Condon, Sean; Stom...
Journal:
Neurology
Issue:
Volume 92:Number 16(2019)
Page Start:
Record Type:
Journal Article
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6. Erratum to "Detection of rarely identified multiple mutations in MECP2 gene do not contribute to enhanced severity in Rett syndrome", Am J Med Genet Part A 161A:1638–1646. Issue 5 (May 2014)

Authors:
Chapleau, Christopher A.; Lane, Jane; Kirwin, Susan; Schanen, Carolyn; Vinette, Kathy M. B.; Stubbolo, Danielle; MacLeod, Patrick; Glaze, Daniel G.; Motil, Kathleen J.; Neul, Jeffrey L.; Skinner, Steven A.; Kaufmann, Walter E.; Percy, Alan K.
Journal:
American journal of medical genetics
Issue:
Volume 164:Issue 5(2014.)
Page Start:
1346
Record Type:
Journal Article
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7. Hand stereotypies: Lessons from the Rett Syndrome Natural History Study. (28th May 2019)

Authors:
Stallworth, Jennifer L.; Dy, Marisela E.; Buchanan, Caroline B.; Chen, Chin-Fu; Scott, Alexandra E.; Glaze, Daniel G.; Lane, Jane B.; Lieberman, David N.; Oberman, Lindsay M.; Skinner, Steven A.; Tierney, Aubin E.; Cutter, Gary R.; Percy, Alan K.; Neul, Jeffrey L.; Kaufmann, Walter E.
Journal:
Neurology
Issue:
Volume 92:Number 22(2019)
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Record Type:
Journal Article
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9. Improving Treatment Trial Outcomes for Rett Syndrome: The Development of Rett-specific Anchors for the Clinical Global Impression Scale. (November 2015)

Authors:
Neul, Jeffrey L.; Glaze, Daniel G.; Percy, Alan K.; Feyma, Tim; Beisang, Arthur; Dinh, Thuy; Suter, Bernhard; Anagnostou, Evdokia; Snape, Mike; Horrigan, Joseph; Jones, Nancy E.
Journal:
Journal of child neurology
Issue:
Volume 30:Number 13(2015:Nov.)
Page Start:
1743
Record Type:
Journal Article
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